Nox Filter Tube Connector 552110

GUDID 15694311110064

Nox Medical ehf.

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Primary Device ID15694311110064
NIH Device Record Keybfd58b80-0d8e-4bcf-8105-8fed311c963f
Commercial Distribution StatusIn Commercial Distribution
Brand NameNox Filter Tube Connector
Version Model NumberNOX-FTC50
Catalog Number552110
Company DUNS365741462
Company NameNox Medical ehf.
Device Count50
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com
Phone999-999-9999
Emailsupport@noxmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS115694311110064 [Primary]
GS115694311111085 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MNRVentilatory Effort Recorder

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-16

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